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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490789Generated: October 29, 2026

HCID 62491089, compound → HCID 178431092, compound

https://huagongshe.com/reaction/1490789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 62491089HCID 62491089—
ReagentBis(pinacolato)diboraneHCID 2733548—
ReagentTetrabutylazanium {5'-methyl-[2,2'-bipyridin]-5-yl}methanesulfonateHCID 165587889—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178431049HCID 17843104913%
ProductHCID 178431092HCID 17843109277%

Reaction Conditions

Temperature35 °C

Reaction Steps

Following general procedure F using 4m (54.5 mg, 0.25 mmol), B2pin2 (95.2 mg, 0.375 mmol), [Ir(COD)OMe]2 (2.5 mg, 0.00375 mmol) and 1a (3.8 mg, 0.0075 mmol) in THF (1.25 mL). Stirred in vial at 35 °C for 6 hours. Analysis of crude 1 H NMR using internal standard 1,2‐dimethoxyethane showed 6.1:1:0.3 meta:para:di(3,5) borylation (overall meta:para borylation 4.7:1)  in 94% yield. Purification by silica gel chromatography proved not to be possible, leading to product decomposition. As such, the compounds were characterised from the crude, which contained pinacol borane impurity, and NMR yield was quoted in manuscript.

Provenance & Evidence

DOI10.1002/anie.201708967
Source datasetBorylation dataset from Roche
ORD IDord-b47e5563af714079860cde41a9dfb09c
Source noteBorylation dataset from Roche